EP2774962B1 - Viskositätsregler für Dispersion mit hoher Konzentration an feinen anorganischen Teilchen und Dispersion mit hoher Konzentration an feinen anorganischen Teilchen enthaltend denselben - Google Patents

Viskositätsregler für Dispersion mit hoher Konzentration an feinen anorganischen Teilchen und Dispersion mit hoher Konzentration an feinen anorganischen Teilchen enthaltend denselben Download PDF

Info

Publication number
EP2774962B1
EP2774962B1 EP14156754.5A EP14156754A EP2774962B1 EP 2774962 B1 EP2774962 B1 EP 2774962B1 EP 14156754 A EP14156754 A EP 14156754A EP 2774962 B1 EP2774962 B1 EP 2774962B1
Authority
EP
European Patent Office
Prior art keywords
fine particles
inorganic fine
high concentration
viscosity modifier
dispersion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP14156754.5A
Other languages
English (en)
French (fr)
Other versions
EP2774962A2 (de
EP2774962A3 (de
Inventor
Daisuke Shimizu
Junpei Suetou
Chihiro Hamazaki
Kenichi Asano
Hideki Satake
Eiichi Sato
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kusumoto Chemicals Ltd
Original Assignee
Kusumoto Chemicals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kusumoto Chemicals Ltd filed Critical Kusumoto Chemicals Ltd
Publication of EP2774962A2 publication Critical patent/EP2774962A2/de
Publication of EP2774962A3 publication Critical patent/EP2774962A3/de
Application granted granted Critical
Publication of EP2774962B1 publication Critical patent/EP2774962B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D171/02—Polyalkylene oxides
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/10—Printing inks based on artificial resins
    • C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D17/00—Pigment pastes, e.g. for mixing in paints
    • C09D17/002—Pigment pastes, e.g. for mixing in paints in organic medium
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/43—Thickening agents

Definitions

  • This invention relates to a viscosity modifier for high concentration dispersion of inorganic fine particles (e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles) and also to a high concentration dispersion of inorganic fine particles which contains the same.
  • inorganic fine particles e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles
  • this invention relates to a viscosity modifier for high concentration dispersion of inorganic fine particles which is liquid and fluid and is therefore handleable, and which can reduce, when blended with a high concentration dispersion of inorganic fine particles to be printed or applied onto various kinds of components or substrates, the occurrence of deformation or distortion at the edge of print or coating, or the occurrence of inconvenience caused by the insufficient thickness of coating film made by printing or coating, and also to a high concentration dispersion of inorganic fine particles which contains the same.
  • This invention further relates to a viscosity modifier for paint composition of high concentration dispersion of inorganic fine particles which, when blended with a paint composition of high concentration dispersion of inorganic fine particles, can prevent the precipitation and hard caking of inorganic fine particles without causing the excess increase of viscosity or giving excess thixotropy, or, in particular, when blended with an inorganic zinc rich paint, can prevent the formation of voids in coating film and can provide uniform surface of coating film, thus making it possible to inhibit the generation of bubbles without mist coat, and also to a paint composition of high concentration dispersion of inorganic fine particles which has been prepared with said viscosity modifier.
  • Dispersion of inorganic fine particles has been used as printing ink or functional paste which is used in the steps for the manufacture of, for example, capacitor, inductor, electronic circuit, electrode, secondary battery, fuel cell, ceramics and display, in the field of electronic materials, or as a part of starting materials to be blended, in the field of general industrial paint or ink.
  • a dispersion of inorganic fine particles makes it possible to precisely control the machining of electronic materials.
  • dispersion of inorganic fine particles has been industrially utilized as a method to contribute to the high performance and mass production of electronic materials.
  • a circuit pattern can easily be formed on a base if circuit is printed with a screen printing method by use of a conductive coating liquid which contains metal fine particles dispersed therein.
  • a protective layer or an insulating layer having a large area can be formed easily by the application, with a coater, of a coating liquid which contains metal oxide particles dispersed therein.
  • the fluidity of the dispersion of fine particles has sometimes caused the deformation or distortion at the edge of print or coating.
  • the fluidity of a dispersion of fine particles has also caused a problem as insufficient thickness of printed film or of coating film.
  • thixotropy which is used herein means the property that, when viscosity is measured with a rotational viscometer for example, low viscosity is indicated at a high rotation (high strain rate) and high viscosity is indicated at a low rotation (low strain rate).
  • Patent Document 1 uses, as a thixotropic agent by which to keep the shape of circuit pattern, fatty amide wax, fumed silica and organic bentonite. When added in a large amount, however, these thixotropic agents may cause clogging in a mesh screen since they are solid particles. Furthermore, fumed silica which is an inorganic substance and organic bentonite are hard to be removed in calcination process.
  • the thixotropic agent not containing solid particles which is disclosed in Patent Document 2 has a high solvent content. Thus produced dispersion of fine particles has therefore sometimes caused inconveniences due to the solvent of thixotropic agent, such as the mixing of other solvents or the decrease of content of fine particles.
  • zinc rich paint which is an industrial paint is a high concentration dispersion of zinc powders.
  • zinc rich paint contains a conventional viscosity modifier such as fatty amide wax, fumed silica and organic bentonite.
  • said conventional rheology modifier often causes excess increase in viscosity when imparting high thixotropy which is necessary in order to prevent precipitation sufficiently.
  • Coating film made from inorganic zinc rich paint has usually a large number of voids.
  • air in the voids causes defects in coating film such as bubbling and pin hole.
  • a so-called "mist coat step” which comprises applying a low viscosity liquid which has been prepared by diluting the base coat paint with a large amount of solvent, with a view to expelling air from the voids of the coating film of inorganic zinc rich paint.
  • the above-mentioned mist coat does not, however, overcome the above-mentioned defects completely. Also from the viewpoint of workload reduction, it has been required to inhibit the occurrence of bubbling without a mist coat step (Patent Document 3).
  • Patent Document 4 discloses an inorganic zinc paint composition which comprises a silicate vehicle, zinc powder and a flake pigment.
  • a coating film is formed by using this paint composition, the flake pigment is distributed selectively in the surface layer of the coating film.
  • solvent cannot reach the voids and replace air in the voids, and, thus, the formation of bubble or pinhole in the coating film can be prevented.
  • WO 2004/048484 A1 describes a rheology control additive for solvent based coating and ink formulations comprising an overbased carboxylate or sulfonate in combination with a hydrocarbyl succinic anhydride based dispersant.
  • the combination of dispersant with carboxylate or sulfonate offers proportionately less viscosity decrease at elevated temperatures and control of viscosity under various shear rates.
  • US 2009/176925 A1 describes a dispersing agent that contains a water-soluble polymer that has excellent dispersibility and stability over time even for a high concentration of a dispersoid such as a pigment and can give a pigment slurry having stable viscosity characteristics and redispersibility due to a large dispersion stabilization effect.
  • the document describes a dispersing agent containing a water-soluble polymer and/or an alkali metal salt or an ammonium salt of the water-soluble polymer, the water-soluble polymer containing (A) an ethylenically unsaturated monocarboxylic acid monomer or an anhydride thereof, or an ethylenically unsaturated dicarboxylic acid monomer or an anhydride thereof, and (B) a polyether compound, a ratio [(B)/(A)] of the number of moles of alkylene oxide added in component (B) relative to the number of moles of carboxyl group in component (A) being no greater than 0.6, and component (B) being less than 25 wt % relative to the total amount.
  • WO 00/39190 A1 describes the synthesis of water-dispersible solid epoxy phosphate ester resins suitable for the formulation of zero VOC water-borne heat-curable coating systems.
  • the solid epoxy phosphate ester resins which can be manufactured without any solvent being present can subsequently be used in solid form or molten form; or the resins can be molten and dispersed in water without the aid of an organic solvent or any other volatile coalescing agent.
  • the solid epoxy phosphate ester resins can be used in ultralow VOC water-borne heat-curable coating systems or in powder coating applications.
  • the purpose of this invention is to provide a viscosity modifier for high concentration dispersion of inorganic fine particles (hereinafter sometimes referred to as viscosity modifier) which is liquid and fluid and is therefore handleable, and can reduce by giving excellent viscosity modifying function, when blended with a high concentration dispersion of inorganic fine particles to be printed or applied onto various kinds of components or substrates, the occurrence of deformation or distortion at the edge of printed film or coating film which has thus been printed or coated in a printing step or coating step for the manufacture of parts, or the occurrence of inconvenience caused by the insufficient thickness of coating film made by printing or coating, and also to a high concentration dispersion of inorganic fine particles which comprises said viscosity modifier (hereinafter sometimes referred to as a high concentration dispersion).
  • viscosity modifier for high concentration dispersion of inorganic fine particles
  • Another purpose of this invention is to provide a viscosity modifier for paint composition of high concentration dispersion of inorganic fine particles which, when blended with a paint composition of high concentration dispersion of inorganic fine particles such as zinc rich paint, can prevent by giving excellent viscosity modifying function the precipitation and hard caking of inorganic fine particles without causing the excess increase of viscosity or giving excess thixotropy, or, in particular, when blended with an inorganic zinc rich paint, can prevent the formation of voids in coating film and can form uniform surface of coating film, thus making it possible to inhibit the occurrence of bubbles without mist coat, and also a paint composition of high concentration dispersion of inorganic fine particles which comprises said viscosity modifier.
  • a reaction product having 2 to 20 phosphate groups or carboxyl groups in a molecular structure which is produced by a reaction between a polyol having two to six hydroxyl groups and a phosphate group-introducing material or a carboxyl group-introducing material at a molar ratio of hydroxyl group to phosphate group-introducing material or carboxyl group-introducing material of 3:1 to 1:1, wherein said carboxyl group-introducing material is selected from the group of succinic acid, succinic anhydride, maleic acid, maleic anhydride, phthalic acid, phthalic anhydride, malic acid, tartaric acid, citric acid and isocitric acid, is useful as a viscosity modifier which has physical bonding force among inorganic fine particles, compatibility with binder and fluidity at normal temperature.
  • the inventors further compounded this viscosity modifier in a high concentration dispersion of inorganic fine particles which comprises inorganic fine particles and binder as essential components (e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles) at a proportion of 0.1 to 15 % by weight, and have thus achieved the above-mentioned purposes.
  • a high concentration dispersion of inorganic fine particles which comprises inorganic fine particles and binder as essential components (e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles) at a proportion of 0.1 to 15 % by weight, and have thus achieved the above-mentioned purposes.
  • the part of acid functional group of the viscosity modifier adsorbs onto the surface of inorganic fine particles, and the viscosity modifier structurally causes physical association of inorganic fine particles since it has plural adsorption sites.
  • an interaction among the physically associated aggregates of inorganic fine particles occurs, and, thus, viscosity modifying function is exhibited (see the attached Figure 1 ).
  • the viscosity modifier of this invention when added to a high concentration dispersion of inorganic fine particles, can reduce the occurrence of deformation or distortion at the edge of printed film or coating film which has thus been printed or coated in a printing step or coating step for the manufacture of parts, or the occurrence of inconvenience caused by the insufficient thickness of coating film made by printing or coating.
  • the viscosity modifier of this invention when added to a paint composition of high concentration dispersion of inorganic fine particles, can prevent the precipitation and hard caking of inorganic fine particles without causing the excess increase of viscosity or giving excess thixotropy, or, in particular, when added to an inorganic zinc rich paint, can prevent the formation of voids in coating film and can form uniform surface of coating film, thus making it possible to inhibit the occurrence of bubbles without mist coat.
  • Figure 1 is a drawing to show the concept of action of the viscosity modifier of this invention.
  • the viscosity modifier of this invention is a reaction product having 2 to 20 phosphate groups or carboxyl groups in molecular structure, which is produced by a reaction between a polyol (e.g., polyhydric alcohol, polyether polyol, and polyester polyol) having two to six hydroxyl groups and a phosphate group-introducing material or a carboxyl group-introducing material at a molar ratio of hydroxyl group to phosphate group-introducing material or carboxyl group-introducing material of 3:1 to 1:1, wherein said carboxyl group-introducing material is selected from the group of succinic acid, succinic anhydride, maleic acid, maleic anhydride, phthalic acid, phthalic anhydride, malic acid, tartaric acid, citric acid and isocitric acid.
  • a polyol e.g., polyhydric alcohol, polyether polyol, and polyester polyol
  • a phosphate group-introducing material or a carboxyl group-introducing material at a m
  • Phosphate group-introducing material in this invention means a material which, when reacting with other materials, can introduce phosphate group in the molecules of reaction product.
  • Carboxyl group-introducing material means a material which, when reacting with other materials, can introduce carboxyl group in the molecules of reaction product.
  • the viscosity modifier of this invention is characterized by being able to physically associate with inorganic fine particles, compatibile with binder and being fluid at normal temperature.
  • This viscosity modifier can be easily added to a high concentration dispersion of inorganic fine particles (e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles) by an easy method without any particular pretreatment.
  • polyhydric alcohol When polyhydric alcohol is to be used as polyol having two to six hydroxyl groups, it may be exemplified by ethylene glycol, propylene glycol, 1,3-propane diol, 1,2-butane diol, 1,4-butane diol, 1,5-pentane diol, 1,2-hexane diol, 3-methyl-1,5-pentane diol, 1,6-hexane diol, 1,7-heptane diol, glycerin, polyglycerin, 1,2,4-butanetriol, trimethylol ethane, trimethylol ethane, trimethylol propane, pentaerythritol, sorbitol, etc.
  • polyether polyol When polyether polyol is to be used as polyol having two to six hydroxyl groups, it may be exemplified by (co)polymer or the like which is produced by the addition reaction of a combination of one, two or more species of the above-mentioned polyhydric alcohols, ethylene oxide, propylene oxide and butylene oxide.
  • polyester polyol When polyester polyol is to be used as polyol having two to six hydroxyl groups, it may be exemplified by (co)polymer or the like which is produced by the reaction of one, two or more species of the above-mentioned polyhydric alcohols; monobasic or polybasic acid such as succinic acid, maleic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, sebacic acid, phthalic acid, terephthalic acid, isophthalic acid, 12-hydroxystearic acid, dimethylolpropionic acid, dimethylolbutyric acid, malic acid, tartaric acid and citric acid; and lactones such as ⁇ -caprolactone and ⁇ -valerolactone.
  • monobasic or polybasic acid such as succinic acid, maleic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, sebacic acid, phthalic acid, tere
  • Phosphate group-introducing material is exemplified by phosphoric acid, pyrophosphoric acid, polyphosphoric acid, phosphorus oxychloride, diphosphorus pentaoxide, etc., which are phosphorus compounds which can form phosphoric ester by reacting with polyol.
  • Carboxyl group-introducing material is selected from the group consisting of succinic acid, succinic anhydride, maleic acid, maleic anhydride, phthalic acid, phthalic anhydride, malic acid, tartaric acid, citric acid and isocitric acid, which are a polybasic acid that can react with polyol.
  • the ratio of hydroxyl group to phosphate group-introducing material or carboxyl group-introducing material in the reaction should be 3:1 to 1:1 (molar ratio).
  • the product from said reaction has 2 to 20 phosphate groups or carboxyl groups in molecular structure.
  • the viscosity modifier of this invention may contain organic solvents so that deposition may be inhibited at a low temperature or that the viscosity modifier may be easily added to a high concentration dispersion of inorganic fine particles.
  • Organic solvent to be used may be aliphatic hydrocarbon, alicyclic hydrocarbon, aromatic hydrocarbon, ketone, ester, alcohol, ether, polyglycol, terpene, etc. It is desirable that solvent which is suitable for the system employed is chosen.
  • Organic solvent is exemplified by methanol, ethanol, normal propyl alcohol, isopropyl alcohol, normal butyl alcohol, isobutyl alcohol, pentyl alcohol, hexyl alcohol, heptyl alcohol, octyl alcohol, 2-ethylhexyl alcohol, ethyleneglycol monomethyl ether, diethyleneglycol monomethyl ether, triethyleneglycol monomethyl ether, ethyleneglycol monoisopropyl ether, diethyleneglycol monoisopropyl ether, triethyleneglycol monoisopropyl ether, ethyleneglycol monobutyl ether, diethyleneglycol monobutyl ether, triethyleneglycol monobutyl ether, propyleneglycol monomethyl ether, dipropyleneglycol monomethyl ether, ethylacetate, normal propylacetate, isopropylacetate, normal butylacetate, isobutylacetate, hexylacetate, ethylene
  • High concentration dispersion of inorganic fine particles e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles
  • the high concentration dispersion of inorganic fine particles of this invention comprises inorganic fine particles, binder and viscosity modifier as essential components. These components are desirably chosen according to the purpose of use of the dispersion.
  • inorganic fine particles include gold, silver, copper, iron, cobalt, aluminum, nickel, tin, zinc, lead, carbon, tungsten, rare earth metal, alloy of said metals, alumina, silica, zirconia, yttria, ferrite, zinc oxide, titanium oxide, talc, calcium carbonate, barium sulfate, barium titanate, lead zirconate titanate, boron oxide, boron nitride, silicon nitride, tungsten carbide, silicon carbide, etc. These may be used singly or in combination, but need to be chosen according to the purpose of use of the high concentration dispersion.
  • the content of inorganic fine particles in the high concentration dispersion of inorganic fine particles of this invention is not limited in particular.
  • the lower limit is 30 % by weight
  • the upper limit is 95 % by weight.
  • the content of inorganic fine particles is less than 30 % by weight, thus obtained high concentration dispersion would have insufficient viscosity, resulting in poor printability or coatability.
  • the content of inorganic fine particles of a paint composition is less than 30 % by weight, thus obtained coating film might give insufficient performance.
  • the content of inorganic fine particles is more than 95 % by weight, thus obtained high concentration dispersion might have too increased viscosity, resulting in poor printing property or application property.
  • Binder is exemplified by ethylcellulose resin, acrylic resin, poly(vinyl butyral) resin, polyvinyl acetal resin, vinylchloride resin, epoxy resin, polyurethane resin, alkyd resin, polyester resin, melamine resin, silicone resin, silicate resin, phenol resin, etc. These may be used singly or in combination, but need to be chosen according to the purpose of use of the high concentration dispersion.
  • the content of binder in the printing ink composition or the functional paste of high concentration dispersion of inorganic fine particles of this invention is not limited in particular.
  • the lower limit is 0.5 % by weight
  • the upper limit is 30 % by weight.
  • the content of binder is less than 0.5 % by weight, thus obtained high concentration dispersion would have too high viscosity, resulting in the decrease of prints.
  • the content of binder is more than 30 % by weight, thus obtained high concentration dispersion might have insufficient viscosity, resulting in poor storage stability or even the precipitation of inorganic fine particles.
  • the content of binder in the paint composition of high concentration dispersion of inorganic fine particles of this invention is not limited in particular.
  • the lower limit is 5 % by weight
  • the upper limit is 60 % by weight.
  • the content of binder is less than 5 % by weight, thus obtained paint composition of high concentration dispersion of inorganic fine particles would have poor coatability.
  • the content of binder is more than 60 % by weight, thus obtained paint composition of high concentration dispersion of inorganic fine particles might fail to give good performance of coating film.
  • the high concentration dispersion of inorganic fine particles of this invention may comprise not only inorganic fine particles, binder and viscosity modifier, but also organic solvents with which to modify the viscosity of the high concentration dispersion.
  • Said organic solvent is exemplified by methanol, ethanol, normal propyl alcohol, isopropyl alcohol, normal butyl alcohol, isobutyl alcohol, pentyl alcohol, hexyl alcohol, heptyl alcohol, octyl alcohol, 2-ethylhexyl alcohol, benzyl alcohol, ethyleneglycol monomethyl ether, diethyleneglycol monomethyl ether, triethyleneglycol monomethyl ether, ethyleneglycol monoisopropyl ether, diethyleneglycol monoisopropyl ether, triethyleneglycol monoisopropyl ether, ethyleneglycol monobutyl ether, diethyleneglycol monobutyl ether, triethyleneglycol monobutyl ether, propyleneglycol monomethyl ether, dipropyleneglycol monomethyl ether, ethylacetate, normal propylacetate, isopropylacetate, normal butylacetate, isobutylacetate,
  • the content of organic solvent is not limited in particular, but preferably falls in a range of 0 to 70 % by weight based on the weight of the high concentration dispersion of inorganic fine particles (e.g., printing ink composition, functional paste composition or paint composition, of high concentration dispersion of inorganic fine particles).
  • the content of organic solvent is more than 70 % by weight, thus obtained high concentration dispersion of inorganic fine particles might have insufficient viscosity, resulting in poor printability or coatability.
  • the high concentration dispersion of inorganic fine particles of this invention may comprise not only inorganic fine particles, binder and viscosity modifier, but also a dispersant with which to facilitate the dispersion of inorganic fine particles.
  • Said dispersant is not limited in particular, so long as inorganic fine particles are thereby dispersed in a medium.
  • amine compound such as octylamine, hexylamine and oleylamine
  • sulfur compound such as dodecane thiol
  • carboxylic compound such as oleic acid
  • branched polymer having ammonium group low molecular or high molecular compound having dithiocarbamate
  • spheric dendritic polymer called dendrimer hyperbranched polymer
  • hyperbranched polymer having ammonium group at the molecular terminal or dispersants on the market such as phosphoric ester dispersant and polyethyleneimine graft polymer dispersant.
  • These dispersants may be used singly or in combination of two or more species.
  • the high concentration dispersion of inorganic fine particles of this invention may further comprise other materials such as surfactant, leveling agent, flame retardant, adhesion improver, coloring agent, antistatic agent, antioxidant, photostabilizer, peeler and coupling agent, as far as the special properties of the dispersion of this invention or the purpose of this invention is not thereby affected.
  • the high concentration dispersion of inorganic fine particles of this invention can be manufactured by the mixing, kneading and dispersing of inorganic fine particles, binder, viscosity modifier, and optionally other necessary components.
  • the step of kneading can be carried out by a conventional method. Kneading apparatus is exemplified by Henschel Mixer, ribbon mixer, planetary mixer, Nauta mixer, paddle mixer, high speed flow type mixer, dissolver, paint shaker, roll mill, ball mill, attritor, sand mill, beads mill, etc.
  • the purpose of use of the high concentration dispersion of inorganic fine particles of this invention is not limited in particular.
  • the same can be used conveniently in printing predetermined patterns of wiring, electrode, resistor, capacitor, coil, etc., in the manufacture of electronic materials such as LED backlight, capacitor, inductor, electronic circuit, conductive adhesive, electrode, secondary battery, fuel cell, laminated ceramics capacitor, plasma display panel, VDF panel, inorganic EL, solar battery panel, microstrip antenna, etc., or in coating electronic materials with a view to giving special function to the same.
  • a 500-mL four neck flask equipped with agitator, temperature adjuster, distributor and nitrogen introduction pipe was filled with 230 parts of propyleneoxide-ethyleneoxide copolymer ("Adeka Pluronic® L-44", a product of ADEKA Corporation having a number average molecular weight of 2200; hydroxyl groups account for 0.2091 mole) and 9.9 parts of diphosphorus pentaoxide (0.0698 mole), which were allowed to react at 120°C for four hours.
  • reaction product is to be called Viscosity Modifier P-1.
  • the molar ratio of hydroxyl group to phosphate group-introducing material is 3:1.
  • Four to five phosphate groups exist in the molecular structure, as inferred from the weight average molecular weight obtained by GPC and from the molar ratio of hydroxyl group to phosphate group-introducing material.
  • reaction product is to be called Viscosity Modifier P-2.
  • the molar ratio of hydroxyl group to phosphate group-introducing material is 1.5:1.
  • Three to four phosphate groups exist in the molecular structure, as inferred from the weight average molecular weight obtained by GPC and from the molar ratio of hydroxyl group to phosphate group-introducing material.
  • reaction product is to be called Viscosity Modifier P-3.
  • the molar ratio of hydroxyl group to phosphate group-introducing material is 3:1.
  • a 500-mL four neck flask equipped with agitator, temperature adjuster, distributor and nitrogen introduction pipe was filled with 230 parts of propyleneoxide-ethyleneoxide copolymer ("Adeka Pluronic® L-101", a product of ADEKA Corporation having a number average molecular weight of 3800; hydroxyl groups account for 0.1211 mole) and 8.6 parts of diphosphorus pentaoxide (0.0603 mole), which were allowed to react at 120°C for four hours.
  • reaction product is to be called Viscosity Modifier P-4.
  • the molar ratio of hydroxyl group to phosphate group-introducing material is 1.5:1.
  • Two to three phosphate groups exist in the molecular structure, as inferred from the weight average molecular weight obtained by GPC and from the molar ratio of hydroxyl group to phosphate group-introducing material.
  • a 500-mL four neck flask equipped with agitator, temperature adjuster, distributor and nitrogen introduction pipe was filled with 230 parts of a copolymer of trihydric alcohol, propyleneoxide and ethyleneoxide ("SANNIX® GL-3000", a product of Sanyo Chemical Industries, Ltd., having a number average molecular weight of 3000; hydroxyl groups account for 0.2300 mole) and 10.9 parts of diphosphorus pentaoxide (0.0768 mole), which were allowed to react at 120°C for four hours.
  • SANNIX® GL-3000 a copolymer of trihydric alcohol, propyleneoxide and ethyleneoxide
  • SANNIX® GL-3000 a copolymer of trihydric alcohol, propyleneoxide and ethyleneoxide
  • diphosphorus pentaoxide (0.0768 mole
  • a 500-mL four neck flask equipped with agitator, temperature adjuster, distributor and nitrogen introduction pipe was filled with 266 parts of a polyester diol which is a reaction product of adipic acid and 3-methyl-1,5-pentanediol ("Kuraray Polyol® P-510", a product of KURARAY CO., LTD. having a number average molecular weight of 500; hydroxyl groups account for 1.0640 mole) and 50.3 parts of diphosphorus pentaoxide (0.3545 mole), which were allowed to react at 120°C for four hours.
  • Viscosity Modifier P-6 the molar ratio of hydroxyl group to phosphate group-introducing material is 3:1. Seven to eight phosphate groups exist in the molecular structure, as inferred from the weight average molecular weight obtained by GPC and from the molar ratio of hydroxyl group to phosphate group-introducing material.
  • a 500-mL four neck flask equipped with agitator, temperature adjuster, distributor and nitrogen introduction pipe was filled with 230 parts of a copolymer of trihydric alcohol, propyleneoxide and ethyleneoxide ("SANNIX® GL-3000", a product of Sanyo Chemical Industries, Ltd., having a number average molecular weight of 3000; hydroxyl groups account for 0.2300 mole) and 14.7 parts of citric acid (0.0765 mole), which were allowed to react at 160°C for two hours.
  • SANNIX® GL-3000 a copolymer of trihydric alcohol, propyleneoxide and ethyleneoxide
  • citric acid 0.0765 mole
  • a 500-mL four neck flask equipped with agitator, temperature adjuster, distributor and nitrogen introduction pipe was filled with 270 parts of a copolymer of tetrahydric alcohol and propyleneoxide ("SANNIX® FA-702", a product of Sanyo Chemical Industries, Ltd., having a number average molecular weight of 6000; hydroxyl groups account for 0.1800 mole) and 8.52 parts of diphosphorus pentaoxide (0.0600 mole), which were allowed to react at 120°C for four hours.
  • SANNIX® FA-702 a copolymer of tetrahydric alcohol and propyleneoxide
  • diphosphorus pentaoxide 0.0600 mole
  • Viscosity Modifier P-8 the molar ratio of hydroxyl group to phosphate group-introducing material is 3:1. Thirteen phosphate groups exist in the molecular structure, as inferred from the weight average molecular weight obtained by GPC and from the molar ratio of hydroxyl group to phosphate group
  • Viscosity Modifier P-9 has low fluidity at normal temperature. To increase fluidity, Viscosity Modifier P-9 may be diluted with epoxy resin (jER807®, manufactured by Mitsubishi Chemical Corporation) to a concentration of 80 %. Thus prepared viscosity modifier is to be called Viscosity Modifier P-10.
  • the molar ratio of hydroxyl group to carboxyl group-introducing material is 3:1.6. Seventeen carboxyl groups exist in the molecular structure, as inferred from the weight average molecular weight obtained by GPC and from the molar ratio of hydroxyl group to carboxyl group-introducing material.
  • powdery fatty amide wax (DISPARLON® 6500, manufactured by Kusumoto Chemicals, Ltd.) (R-1), fatty amide paste (DISPARLON® 6900-20X, manufactured by Kusumoto Chemicals, Ltd.) (R-2), fumed silica (AEROSIL® R972, manufactured by Nippon Aerosil Co., Ltd.) (R-3) and fatty amide paste (DISPARLON® 6900-10X, manufactured by Kusumoto Chemicals, Ltd.) (R-4) which had been put on the market were each used as a thixotropic agent.
  • Table-1 shows the content of effective components in the viscosity modifiers of this invention and in those of Comparative Example, and also the appearance of the same.
  • the viscosity modifiers of this invention and the thixotropic agents of the comparative example were subjected to a pyrolytic property test with TG-DTA (DTG-60A manufactured by SHIMADZU CORPORATION) by use of aluminum cell, in nitrogen atmosphere, and at a temperature elevation rate of 10°C/min. In this test, the temperature at which the weight decreased by more than 95 % was recorded as pyrolytic temperature. Results of this test are shown in Table-2.
  • Aluminum fine particles (ALF11PB®, manufactured by Kojundo Chemical Laboratory Co., Ltd.), a terpineol solution of ethylcellulose resin (STD-45®, manufactured by The Dow Chemical Company) and a dispersant (HIPLAAD ED 154®, manufactured by Kusumoto Chemicals, Ltd.) were mixed in accordance with the formulation of Table-3, and the resultant mixture was subjected to a roll mill treatment. Subsequently, a viscosity modifier was added, and the resultant mixture was further passed through a roll mill to give a dispersion of aluminum fine particles.
  • AMF11PB® manufactured by Kojundo Chemical Laboratory Co., Ltd.
  • STD-45® manufactured by The Dow Chemical Company
  • HIPLAAD ED 154® manufactured by Kusumoto Chemicals, Ltd.
  • the viscosity of the above-mentioned aluminum fine particles dispersion was measured with a 3° ⁇ R9.7 mm cone rotor of E-type Viscometer at 25°C.
  • the values of T.I. were given by the ratio of viscosity at a shear rate of 0.4 [1/sec] to viscosity at a shear rate of 4 [1/sec] at temperature of 25°C.
  • the viscosity and T.I. value of the aluminum fine particles dispersion are shown by Table-4 below.
  • An organic solvent (Terpineol C®, manufactured by Nippon Terpene Chemicals, Inc.) was added to the blend of Test Example 2. The resultant mixture was dispersed by the method as mentioned in Test Example 2, to give aluminum fine particles dispersion.
  • Table-5 Special properties of aluminum fine particles dispersion Aluminum content 70 % Aluminum content 50 % Aluminum content 30 % Viscosity Pa ⁇ s T.I. value Viscosity Pa ⁇ s T.I. value Viscosity Pa ⁇ s T.I. value No addition 22.0 0.8 1.09 1.2 0.20 1.2 P-2 27.1 2.1 1.37 1.7 0.20 2.3 P-3 31.9 2.2 1.31 1.8 0.24 1.6 P-4 28.7 1.7 1.61 2.5 0.22 1.4
  • Silver fine particles (AG2-1C®, DOWA Electronics Co., Ltd.) and a terpineol solution of ethylcellulose resin (STD-45®, manufactured by The Dow Chemical Company) were mixed in accordance with the formulation of Table-6, and the resultant mixture was subjected to a roll mill treatment. Subsequently, a viscosity modifier was added, and the resultant mixture was further passed through a roll mill to give a dispersion of silver fine particles.
  • the viscosity of the above-mentioned silver fine particles dispersion was measured with a 3° ⁇ R9.7 mm cone rotor of E-type Viscometer at 25°C.
  • the viscosity and T.I. values of the silver fine particles dispersion are shown by Table-7 below.
  • Thin lines were drawn with thus obtained silver fine particles dispersion on a ceramics substrate by screen printing method with a screen of #400 mesh and a line width of 90 ⁇ m. Special properties of the silver fine particles dispersion were evaluated by the reproducibility of the line width. Results of evaluation are shown in Table-7.
  • Silver fine particles AG2-1C®, DOWA Electronics Co., Ltd.
  • a terpineol solution of acrylic resin manufactured by Kusumoto Chemicals, Ltd.
  • a viscosity modifier was added, and the resultant mixture was further passed through a roll mill to give a dispersion of silver fine particles.
  • the viscosity of the above-mentioned silver fine particles dispersion was measured with a 3° ⁇ R9.7 mm cone rotor of E-type Viscometer at 25°C.
  • the viscosity and T.I. values of the silver fine particles dispersion are shown by Table-9 below.
  • Thin lines were drawn with thus obtained silver fine particles dispersion on a ceramics substrate by screen printing method with a screen of #400 mesh and a line width of 90 ⁇ m. Special properties of the silver fine particles dispersion were evaluated by the reproducibility of the line width. Results of evaluation are shown in Table-9.
  • Fused silica powder (FB-3LDX®, manufactured by Denki Kagaku Kogyo Kabushiki Kaisha), epoxy resin (jER807®, manufactured by Mitsubishi Chemical Corporation) and a viscosity modifier were mixed in accordance with the formulation of Table-10, and the resultant mixture was dispersed with a planetary centrifugal mixer to give a dispersion of fused silica powder.
  • a predetermined amount of viscosity modifier was added to ethyl silicate resin (HAS-1®, manufactured by COLCOAT CO.,Ltd.) in accordance with the formulation of Table-12, and the resultant mixture was dispersed with a dissolver. Subsequently, zinc powder (zinc powder #3, manufactured by Sakai Chemical Industry Co., Ltd.) was mixed, and the resultant mixture was dispersed with a dissolver to give an inorganic zinc rich paint.
  • HAS-1® ethyl silicate resin
  • Table-12 ethyl silicate resin
  • zinc powder zinc powder #3, manufactured by Sakai Chemical Industry Co., Ltd.
  • the viscosity of the above-mentioned inorganic zinc rich paint was measured with a rheometer at 25°C.
  • the values of T.I. were given by the ratio of viscosity at a shear rate of 0.1 [1/sec] to viscosity at a shear rate of 1 [1/sec] at temperature of 25°C.
  • the viscosity and T.I. value of the inorganic zinc rich paint are shown by Table-13 below.
  • the above-mentioned inorganic zinc rich paint was further subjected to a precipitation test in a sealed test bottle.
  • the paint was left to stand still at room temperature for a day, and, after that, the sedimentation volume of zinc powder (the percentage of the volume of sediment of zinc powder to the total volume of paint) was measured.
  • the hardness of zinc powder sediment was tested by the sensory analysis of metal bar invasion resistance, and the obtained results were evaluated according to the five-grade evaluation system from Grade 1 (very hard) to Grade 5 (soft).
  • the sedimentation volume and the sedimentation hardness of inorganic zinc rich paint are shown in Table-13 below.
  • the viscosity modifier of this invention prevents the sedimentation of inorganic fine particles and thus exhibits good effects of preventing hard caking without causing the excess increase of viscosity or giving excess thixotropy, as compared with conventional thixotropic agent of comparative example.
  • the above-mentioned inorganic zinc rich paint was applied on a glass plate with a 250 ⁇ m-applicator.
  • coated plate was dried at room temperature (20°C) for seven days, and, then, the coating film surface was observed with a laser microscope.
  • Surface roughness (Ra: arithmetic average roughness; Ry: maximum height) was obtained from an average of five measurement points with no filter processing, on the basis of JIS B 0601.
  • 3D observation of the unevenness of coating film surface was made with a laser microscope, and, then, the porosity of coating film surface was evaluated with visual observation according to the five-grade evaluation system from Grade 1 (highly porous) to Grade 5 (no pores at all).
  • Ra, Ry and the porosity of coating film surface of inorganic zinc rich paint are shown in Table-15.
  • Epoxy paint of Table-14 was applied on coating film of the above-mentioned inorganic zinc rich paint with a 250 ⁇ m-applicator, and was then dried at room temperature for one day.
  • the state of foam and pin holes which had been generated on the epoxy coating film of thus obtained test plate was evaluated according to the five-grade evaluation system from Grade 1 (remarkable foaming) to Grade 5 (no foaming). The result of evaluation is shown in Table-15.
  • the viscosity modifier of this invention is expected to contribute to the improvement in high performance and mass production of electronic materials when predetermined patterns of wiring, electrode, resistor, capacitor, coil, etc., are to be printed with ink or functional paste in the manufacture of electronic materials (e.g., LED backlight, capacitor, inductor, electronic circuit, conductive adhesive, electrode, secondary battery, fuel cell, laminated ceramics capacitor, plasma display panel, VDF panel, inorganic EL, solar battery panel, microstrip antenna, etc.), or when electronic materials are to be coated with paint so that special function may be given to the same.
  • electronic materials e.g., LED backlight, capacitor, inductor, electronic circuit, conductive adhesive, electrode, secondary battery, fuel cell, laminated ceramics capacitor, plasma display panel, VDF panel, inorganic EL, solar battery panel, microstrip antenna, etc.
  • the viscosity modifier of this invention is expected to contribute to the prevention of the precipitation of pigment or inorganic fine particles, or to the improvement of performance of coating film or print film.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Paints Or Removers (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Claims (7)

  1. Viskositätsmodifiziermittel für eine Dispersion anorganischer feiner Partikel mit hoher Konzentration, das ein Reaktionsprodukt mit 2 bis 20 Phosphatgruppen oder Carboxylgruppen in der Molekülstruktur umfasst, wobei das Reaktionsprodukt aus einer Reaktion zwischen einem Polyol mit zwei bis sechs Hydroxylgruppen und einem Phosphatgruppe-einführenden Material oder einem Carboxylgruppe-einführenden Material bei einem molaren Verhältnis von Hydroxylgruppe zu Phosphatgruppe-einführendem Material oder Carboxylgruppe-einführendem Material von 3:1 bis 1:1 hergestellt ist, wobei das Carboxylgruppe-einführende Material aus der Gruppe aus Bernsteinsäure, Bernsteinsäureanhydrid, Maleinsäure, Maleinsäureanhydrid, Phthalsäure, Phthalsäureanhydrid, Äpfelsäure, Weinsäure, Citronensäure und Isocitronensäure ausgewählt ist.
  2. Viskositätsmodifiziermittel gemäß Anspruch 1, wobei die Dispersion anorganischer feiner Partikel mit hoher Konzentration eine Drucktintenzusammensetzung ist.
  3. Viskositätsmodifiziermittel gemäß Anspruch 1, wobei die Dispersion anorganischer feiner Partikel mit hoher Konzentration eine funktionelle Pastenzusammensetzung ist.
  4. Viskositätsmodifiziermittel gemäß Anspruch 1, wobei die Dispersion anorganischer feiner Partikel mit hoher Konzentration eine Farbzusammensetzung ist.
  5. Drucktintenzusammensetzung, die anorganische feine Partikel, ein Bindemittel und das Viskositätsmodifiziermittel gemäß Anspruch 1 umfasst.
  6. Funktionelle Pastenzusammensetzung, die anorganische feine Partikel, ein Bindemittel und das Viskositätsmodifiziermittel gemäß Anspruch 1 umfasst.
  7. Farbzusammensetzung, die anorganische feine Partikel, ein Bindemittel und das Viskositätsmodifiziermittel gemäß Anspruch 1 umfasst.
EP14156754.5A 2013-03-08 2014-02-26 Viskositätsregler für Dispersion mit hoher Konzentration an feinen anorganischen Teilchen und Dispersion mit hoher Konzentration an feinen anorganischen Teilchen enthaltend denselben Active EP2774962B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2013046812 2013-03-08
JP2013261171A JP5755717B2 (ja) 2013-03-08 2013-12-18 無機微粒子高濃度分散体用粘性調整剤及びそれが配合された無機微粒子高濃度分散体

Publications (3)

Publication Number Publication Date
EP2774962A2 EP2774962A2 (de) 2014-09-10
EP2774962A3 EP2774962A3 (de) 2014-12-24
EP2774962B1 true EP2774962B1 (de) 2018-10-03

Family

ID=50156669

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14156754.5A Active EP2774962B1 (de) 2013-03-08 2014-02-26 Viskositätsregler für Dispersion mit hoher Konzentration an feinen anorganischen Teilchen und Dispersion mit hoher Konzentration an feinen anorganischen Teilchen enthaltend denselben

Country Status (6)

Country Link
US (1) US9464208B2 (de)
EP (1) EP2774962B1 (de)
JP (1) JP5755717B2 (de)
KR (1) KR101632780B1 (de)
CN (1) CN104031464B (de)
TW (1) TWI504703B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104505265B (zh) * 2014-12-08 2018-03-16 西安交通大学 一种采用3d打印技术制造微型超级电容器的方法
KR101660681B1 (ko) * 2015-01-27 2016-09-27 데이코쿠 잉키 세이조 가부시키가이샤 고품위·고정밀 스크린 인쇄용 잉크 조성물, 해당 잉크 조성물을 스크린 인쇄한 인쇄물 및 해당 인쇄물의 제조 방법
US20170283629A1 (en) * 2016-03-29 2017-10-05 University Of North Texas Metal-based ink for additive manufacturing process
DE102016206345A1 (de) * 2016-04-15 2017-10-19 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Pastöse Zusammensetzung sowie ein Verfahren zum Herstellen von dreidimensionalen Strukturen oder Strukturelementen auf Substratoberflächen
JP7011611B2 (ja) * 2019-01-28 2022-02-10 富士フイルム株式会社 内視鏡用コーティング組成物、内視鏡用潤滑性部材、内視鏡用潤滑性部材の製造方法、内視鏡用可撓管、及び内視鏡
WO2021099233A1 (en) 2019-11-18 2021-05-27 Merck Patent Gmbh Method for fabricating a particle
WO2021099351A1 (en) 2019-11-21 2021-05-27 Merck Patent Gmbh Method for fabricating a particle
WO2022013049A1 (en) 2020-07-13 2022-01-20 Merck Patent Gmbh Method for fabricating a particle

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58167470A (ja) * 1982-03-25 1983-10-03 第一工業製薬株式会社 セラミツク用バインダ−
JPS5951951A (ja) 1982-09-17 1984-03-26 Hitachi Zosen Corp 無機質亜鉛塗料組成物
GB9609436D0 (en) * 1996-05-04 1996-07-10 Zeneca Ltd Composition and use
US6043300A (en) * 1996-12-09 2000-03-28 Rheox, Inc. Liquid rheological additives for non-aqueous systems and non-aqueous systems containing such liquid rheological additives
WO2000039190A1 (en) 1998-12-23 2000-07-06 The Dow Chemical Company Solid polyhydroxy polyether phosphate ester compositions
JP2002146336A (ja) 2000-11-15 2002-05-22 Kusumoto Kasei Kk アマイド系ペースト状チクソトロピック剤
JP4444490B2 (ja) 2000-12-26 2010-03-31 関西ペイント株式会社 無機質ジンクリッチペイント
JP2003151351A (ja) 2001-08-30 2003-05-23 Kyocera Corp 導電性ペースト及びセラミック回路基板の製法
CA2506631A1 (en) 2002-11-21 2004-06-10 The Lubrizol Corporation Compositions comprising a dispersant and an overbased carboxylate or sulfonate for rheology control in coatings and inks
JP4050752B2 (ja) * 2005-02-24 2008-02-20 東芝テック株式会社 インクジェットインク、および印字方法
CN100500773C (zh) * 2005-05-18 2009-06-17 江南大学 一种数字喷墨印花墨水及其制备方法
KR20090018643A (ko) 2006-05-22 2009-02-20 도아고세이가부시키가이샤 분산제
JP4971784B2 (ja) * 2006-12-27 2012-07-11 株式会社リコー インクメディアセット、並びにインクカートリッジ、インクジェット記録方法、インクジェット記録装置、及びインク記録物
JP2010119930A (ja) * 2008-11-18 2010-06-03 Riken Vitamin Co Ltd セラミックス用分散剤
EP2534184B1 (de) * 2010-02-12 2017-09-27 Rhodia Operations Rheologiemodifizierendes polymer
WO2012140202A1 (en) * 2011-04-15 2012-10-18 Basf Se Hyperbranched polyesters in printing inks

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
KR101632780B1 (ko) 2016-07-01
JP5755717B2 (ja) 2015-07-29
US9464208B2 (en) 2016-10-11
EP2774962A2 (de) 2014-09-10
JP2014196466A (ja) 2014-10-16
TWI504703B (zh) 2015-10-21
CN104031464B (zh) 2016-08-31
TW201439241A (zh) 2014-10-16
CN104031464A (zh) 2014-09-10
EP2774962A3 (de) 2014-12-24
KR20140111223A (ko) 2014-09-18
US20140251178A1 (en) 2014-09-11

Similar Documents

Publication Publication Date Title
EP2774962B1 (de) Viskositätsregler für Dispersion mit hoher Konzentration an feinen anorganischen Teilchen und Dispersion mit hoher Konzentration an feinen anorganischen Teilchen enthaltend denselben
KR20070097055A (ko) 도전성 잉크
KR100768341B1 (ko) 금속성 잉크, 그리고 이를 이용한 전극형성방법 및 기판
EP3409729B1 (de) Elektrisch leitfähige zusammensetzung, herstellungsverfahren dafür und elektrisch leitendes material
KR20070065379A (ko) 도전성 잉크
EP2468827A1 (de) Dispersion mit metallischen, Metalloxid- oder Metallvorläufernanopartikeln
WO2013092450A1 (en) A dispersion comprising metallic, metal oxide or metal precursor nanoparticles, a polymeric dispersant and a thermally cleavable agent
EP2383316A2 (de) Transparente farbbeschichtungszusammensetzung mit dispergierten pigmenten in nanoformat, beschichtetes substrat und herstellungsverfahren dafür
EP4036180B1 (de) Metallpigmentzusammensetzung und färbeverfahren
JP6036185B2 (ja) 高純度の金属ナノ粒子分散体ならびにその製造方法
JP2012007144A (ja) 分散体組成物
KR101618093B1 (ko) 도전막 형성을 위한 유연 기판용 전도성 페이스트 조성물 및 이의 제조방법
KR20160120716A (ko) 금속 나노 미립자의 제조 방법
KR20130096307A (ko) 분산제 및 분산체 조성물
TWI512054B (zh) Composition of inkjet containing nickel particles
TWI440672B (zh) ITO ink
KR100728910B1 (ko) 금속성 잉크, 그리고 이를 이용한 전극형성방법 및 기판
CN112424297A (zh) 具有高透明性的无机氧化物分散体
KR102304865B1 (ko) 도전성막 형성용 조성물, 도전성막, 도금막의 제조 방법, 도금막 및 전자 기기
US20110318541A1 (en) Metal ink composition and method for forming the metal line using the same, and conductive pattern formed by using the metal ink composition
US20090176933A1 (en) Method For Production Of Polyester Resins Containing Nanodispersed Nanoscale Additives As Binders For Coating Powers
TW202341185A (zh) 導電性組成物
EP4268998A1 (de) Verfahren zur herstellung eines verbundstoffmaterials
US20220204785A1 (en) Water-Based Composition And Coloring Method
JP2019214650A (ja) 金属ナノ粒子を含有する分散組成物及びその成形体

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20140226

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

RIC1 Information provided on ipc code assigned before grant

Ipc: C09D 11/00 20140101AFI20141114BHEP

R17P Request for examination filed (corrected)

Effective date: 20150317

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20171016

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20180524

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1048563

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181015

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602014033228

Country of ref document: DE

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1048563

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181003

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190103

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190203

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190103

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190104

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190203

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602014033228

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

26N No opposition filed

Effective date: 20190704

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190228

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190226

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190226

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20140226

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181003

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LU

Payment date: 20240220

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20240202

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240222

Year of fee payment: 11

Ref country code: GB

Payment date: 20240118

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20240206

Year of fee payment: 11

Ref country code: FR

Payment date: 20240123

Year of fee payment: 11

Ref country code: BE

Payment date: 20240131

Year of fee payment: 11